Of significance, the tumorigenic CD44+ cell populations in both Du145 and LAPC9 commonly upregulate 14 genes involved in development (FGF1, FGFR1, and DVL1), cell cycle (RB1, CDC2, CCND2, and CCNA2), and neuronal activity (TUBB3 and NEUROG2), providing potential therapeutic targets for the CD44+ PCa cells. The gene discussed is CCNA2; the disease is posterior cortical atrophy.